Prophylactic Cefazolin Dosing and Surgical Site Infections: Does the Dose Matter in Obese Patients?


Journal

Obesity surgery
ISSN: 1708-0428
Titre abrégé: Obes Surg
Pays: United States
ID NLM: 9106714

Informations de publication

Date de publication:
01 2019
Historique:
pubmed: 30 9 2018
medline: 31 12 2019
entrez: 30 9 2018
Statut: ppublish

Résumé

Most surgical prophylaxis guidelines recommend a 3-g cefazolin intravenous dose in patients weighing ≥ 120 kg. However, this recommendation is primarily based on pharmacokinetic studies rather than robust clinical evidence. This study aimed to compare the prevalence of surgical site infections (SSIs) in obese and non-obese patients (body mass index ≥ 30 kg/m A retrospective case-control study was conducted in adult elective surgical patients. Patients receiving 2- g cefazolin were grouped as obese and non-obese, and by weight (≥ 120 kg or < 120 kg). The 90-day prevalence of SSI and potential contributing factors were investigated. We identified 152 obese (median 134 kg) and 152 non-obese control (median 73 kg) patients. Baseline characteristics were similar between groups, except for an increased prevalence in the obese group of diabetes (35.5% vs 13.2%; p < 0.001) and an American Society of Anaesthesiologists Score of 3 (61.8% vs 17.1%; p < 0.001). While not statistically significant, the prevalence of SSI in the obese group was almost double that in the non-obese group (8.6% vs 4.6%; p = 0.25) and in patients weighing ≥ 120 kg (n = 102) compared to those weighing < 120 kg (n = 202) (9.8% vs 5.0%; p = 0.17). The prevalence of SSI was not significantly increased in obese patients, or those weighing ≥ 120 kg, who received cefazolin 2- g prophylactically; however, trends toward an increase were evident. Large-scale randomised trials are needed to examine whether a 2-g or 3-g cefazolin is adequate to prevent SSI in obese (and ≥ 120 kg) individuals.

Sections du résumé

BACKGROUND
Most surgical prophylaxis guidelines recommend a 3-g cefazolin intravenous dose in patients weighing ≥ 120 kg. However, this recommendation is primarily based on pharmacokinetic studies rather than robust clinical evidence. This study aimed to compare the prevalence of surgical site infections (SSIs) in obese and non-obese patients (body mass index ≥ 30 kg/m
METHODS
A retrospective case-control study was conducted in adult elective surgical patients. Patients receiving 2- g cefazolin were grouped as obese and non-obese, and by weight (≥ 120 kg or < 120 kg). The 90-day prevalence of SSI and potential contributing factors were investigated.
RESULTS
We identified 152 obese (median 134 kg) and 152 non-obese control (median 73 kg) patients. Baseline characteristics were similar between groups, except for an increased prevalence in the obese group of diabetes (35.5% vs 13.2%; p < 0.001) and an American Society of Anaesthesiologists Score of 3 (61.8% vs 17.1%; p < 0.001). While not statistically significant, the prevalence of SSI in the obese group was almost double that in the non-obese group (8.6% vs 4.6%; p = 0.25) and in patients weighing ≥ 120 kg (n = 102) compared to those weighing < 120 kg (n = 202) (9.8% vs 5.0%; p = 0.17).
CONCLUSION
The prevalence of SSI was not significantly increased in obese patients, or those weighing ≥ 120 kg, who received cefazolin 2- g prophylactically; however, trends toward an increase were evident. Large-scale randomised trials are needed to examine whether a 2-g or 3-g cefazolin is adequate to prevent SSI in obese (and ≥ 120 kg) individuals.

Identifiants

pubmed: 30267229
doi: 10.1007/s11695-018-3497-0
pii: 10.1007/s11695-018-3497-0
pmc: PMC6320352
doi:

Substances chimiques

Anti-Bacterial Agents 0
Cefazolin IHS69L0Y4T

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

159-165

Références

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Auteurs

Zahid Hussain (Z)

Division of Pharmacy, College of Health and Medicine, University of Tasmania, Hobart, Tasmania, Australia.

Colin Curtain (C)

Division of Pharmacy, College of Health and Medicine, University of Tasmania, Hobart, Tasmania, Australia.

Corinne Mirkazemi (C)

Division of Pharmacy, College of Health and Medicine, University of Tasmania, Hobart, Tasmania, Australia.

Karl Gadd (K)

Department of Anaesthesia, Launceston General Hospital, Launceston, Tasmania, Australia.
Head of Anaesthesia Discipline, Launceston Clinical School, University of Tasmania, Launceston, Tasmania, Australia.

Gregory M Peterson (GM)

Division of Pharmacy, College of Health and Medicine, University of Tasmania, Hobart, Tasmania, Australia.

Syed Tabish R Zaidi (STR)

Division of Pharmacy, College of Health and Medicine, University of Tasmania, Hobart, Tasmania, Australia. S.T.R.Zaidi@leeds.ac.uk.
School of Healthcare, University of Leeds, Leeds, LS2 9JT, UK. S.T.R.Zaidi@leeds.ac.uk.

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